Suppr超能文献

利用人工智能革新CRISPR技术。

Revolutionizing CRISPR technology with artificial intelligence.

作者信息

Kim Min-Gyeong, Go Min-Ji, Kang Seung-Hun, Jeong Soo-Hwan, Lim Kayeong

机构信息

Biomedical Research Division, Korea Institute of Science and Technology, Seoul, Republic of Korea.

Division of Bio-Medical Science and Technology, KIST School, University of Science and Technology, Seoul, Republic of Korea.

出版信息

Exp Mol Med. 2025 Jul;57(7):1419-1431. doi: 10.1038/s12276-025-01462-9. Epub 2025 Jul 31.

Abstract

Genome engineering has made remarkable strides, evolving from DNA-binding proteins such as zinc fingers and transcription activator-like effectors to CRISPR-Cas systems. CRISPR technology has revolutionized the field through its simplicity and ability to target specific genome regions via guide RNA and Cas proteins. Progress in CRISPR tools-CRISPR nucleases, base editors and prime editors-has expanded the toolkit to induce targeted insertions or deletions, nucleotide conversions and a wider array of genetic alterations. Nevertheless, variations in editing outcomes across cell types and unintended off-target effects still present substantial hurdles. Artificial intelligence (AI), which has seen rapid advances, provides high-level solutions to these problems. By leveraging large datasets from diverse experiments, AI enhances guide RNA design, predicts off-target activities and improves editing efficiency. In addition, AI aids in discovering and designing novel CRISPR systems beyond natural limitations. These developments provide new modalities essential for the innovation of personalized therapies and help to ensure efficiency, precision and safety. Here we discuss the transformative role of AI in advancing CRISPR technology. We highlight how AI contributes to refining nuclease-based editing, base editing and prime editing. Integrating AI with CRISPR technology enhances existing tools and opens doors to next-generation medicine for gene therapy.

摘要

基因组工程已经取得了显著进展,从诸如锌指蛋白和转录激活样效应因子等DNA结合蛋白发展到CRISPR-Cas系统。CRISPR技术凭借其简单性以及通过向导RNA和Cas蛋白靶向特定基因组区域的能力,给该领域带来了变革。CRISPR工具(CRISPR核酸酶、碱基编辑器和引导编辑器)的进展扩大了工具集,以诱导靶向插入或缺失、核苷酸转换以及更广泛的基因改变。然而,不同细胞类型间编辑结果的差异以及意外的脱靶效应仍然是巨大的障碍。快速发展的人工智能(AI)为这些问题提供了高级解决方案。通过利用来自各种实验的大型数据集,AI改进了向导RNA设计,预测了脱靶活性并提高了编辑效率。此外,AI有助于发现和设计超越自然限制的新型CRISPR系统。这些进展提供了个性化疗法创新所必需的新方法,并有助于确保效率、精准度和安全性。在此,我们讨论AI在推进CRISPR技术方面的变革性作用。我们强调AI如何有助于改进基于核酸酶的编辑、碱基编辑和引导编辑。将AI与CRISPR技术相结合可增强现有工具,并为基因治疗的下一代医学打开大门。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验